ClinicalTrials.Veeva

Menu

Glucose Monitoring in Tissue Transfers

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Withdrawn

Conditions

Reconstructive Tissue Surgery

Treatments

Device: Continuous glucose monitoring system

Study type

Interventional

Funder types

Other

Identifiers

NCT00962130
H-2008-0066

Details and patient eligibility

About

The purpose of this study is to determine if 1) a continuous glucose monitoring system can measure glucose levels in transferred tissue during reconstructive surgery, and 2) if glucose measurements from a continuous glucose monitoring system correlate with tissue blood perfusion.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • presence of a soft tissue deformity where reconstruction with a pedicled or free tissue transfer is indicated
  • age 18 and over
  • ability to follow-up post-operatively

Exclusion criteria

  • age less than 18
  • prisoner status
  • inability to participate in a standard post-operative follow-up visit

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Blood Glucose Measurement
Experimental group
Description:
Subjects have sensors placed on skin before surgery and these sensors will measure the subject's glucose until the third day after surgery when they are removed.
Treatment:
Device: Continuous glucose monitoring system

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems